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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Plug, Punctum
510(k) Number K050851
Device Name DELTA PUNCTUM PLUG
Applicant
Delta Life Science, Inc.
1975 Nonconnah Blvd.
Memphis,  TN  38132
Applicant Contact GEORGE W MURRAY
Correspondent
Delta Life Science, Inc.
1975 Nonconnah Blvd.
Memphis,  TN  38132
Correspondent Contact GEORGE W MURRAY
Classification Product Code
LZU  
Date Received04/04/2005
Decision Date 08/19/2005
Decision Substantially Equivalent (SESE)
510k Review Panel Ophthalmic
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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